Medical Device Recalls
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1 result found
510(K) Number: K091908 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Cobalt HV Bone Cement Cobalt MV Bone Cement Cobalt HV Bone Cement With Gentamicin | 2 | 04/25/2017 | Zimmer Biomet, Inc. |
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